CN109014239A - A kind of preparation method of touch screen laser ablation silver paste silver powder - Google Patents

A kind of preparation method of touch screen laser ablation silver paste silver powder Download PDF

Info

Publication number
CN109014239A
CN109014239A CN201810886037.7A CN201810886037A CN109014239A CN 109014239 A CN109014239 A CN 109014239A CN 201810886037 A CN201810886037 A CN 201810886037A CN 109014239 A CN109014239 A CN 109014239A
Authority
CN
China
Prior art keywords
solution
touch screen
silver powder
preparation
silver
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201810886037.7A
Other languages
Chinese (zh)
Inventor
曹笃盟
杨荣春
齐勇
马骞
范秀娟
王维斌
孟涛
任哲峥
包飞燕
王媛媛
张亚红
吴婧
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jinchuan Lanzhou Science And Technology Park Co Ltd
Jinchuan Group Co Ltd
Original Assignee
Jinchuan Lanzhou Science And Technology Park Co Ltd
Jinchuan Group Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jinchuan Lanzhou Science And Technology Park Co Ltd, Jinchuan Group Co Ltd filed Critical Jinchuan Lanzhou Science And Technology Park Co Ltd
Priority to CN201810886037.7A priority Critical patent/CN109014239A/en
Publication of CN109014239A publication Critical patent/CN109014239A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/16Making metallic powder or suspensions thereof using chemical processes
    • B22F9/18Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
    • B22F9/24Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions

Abstract

The invention discloses a kind of touch screen preparation methods of laser ablation silver paste silver powder, belong to conductive metal Preparation Technique of Powders field, include the following steps: to prepare reducing agent solution, dispersant solution and metal salt solution, hybrid reaction, washing is separated by solid-liquid separation to obtain filter cake to conductivity≤20ms, and filter cake is dried to moisture content and obtains silver powder less than 0.2%.Preparation method of the invention is easy to operate, and raw material sources are extensive, at low cost, to the of less demanding of equipment;Obtained touch screen is very high with the diameter of particle concentration degree of the preparation method of laser ablation silver paste silver powder, silver powder maximum particle diameter D1005 μm of <, good dispersion.

Description

A kind of preparation method of touch screen laser ablation silver paste silver powder
Technical field
The invention belongs to conductive metal Preparation Technique of Powders fields, and in particular to a kind of touch screen laser ablation silver paste use The preparation method of silver powder.
Background technique
Touch screen originates from the U.S. of the 1960s, is that US military is developed for military use.More than 50 The development in year, touch screen has been widely used, but just actually enters the maturity period after 2000.The first generation in 2007 IPhone mobile phone has pulled open the prelude in smart phone full touch-control epoch, becomes a milestone of touch-control industry development.2010 Year, with the explosive growth of smart phone and being announced to the world splendidly for tablet computer, touch control operation, especially capacitance touching control are operated Core status on intelligent mobile terminal is confirmed.First generation iPad publication, so that touch screen competition is extended from small size To middle large size product market.2012, Samsung emerged in smart phone market, while tablet computer enters the fast growth phase, The heating of ultrabook concept, touch screen field enters the high-speed developing period of product diversification, brand diversification.
Currently, with the continuous development of science and technology, touch screen will be used wider and wider.It is operated from the control of shop equipment System, the electronic equipment of public information inquiry, commercial use ATM, arrive consumer electronics mobile phone, PDA, numerical control phase The figure of touch screen all can be seen in machine etc..According to the related data of market research agency Display Search, the whole world in 2016 Touch screen shipment amount reaches 3,000,000,000 pieces, and business revenue reaches 30,000,000,000 dollars, and the development prospect in touch screen market future is very tempting.But When smart electronic consumer product mobile phone, tablet computer etc. become the carrier of universal information transmission and reading, carrying user information is got over While coming more, people put forward higher requirements touch-control industry again.The electrode silver of one of critical material as touch screen Slurry, it is most direct on touch screen performance influence, and as the requirement for touching precision is higher and higher, silver paste also proposed higher more Harsh technical requirements.
However, the silver paste and silver powder product of mating touch screen domestic at present are almost blank, 95% or more all rely on into Mouthful.And have two side's production methods at present for touch screen silver paste electrode circuit, first is that using traditional silk-screen printing technique in ITO Surface printing electronic circuit, this is current preparation contact electrode and the widely used technology of conducting wire;Second is that being lost by laser It carves, the touch screen made using laser ablation is linear preferably, without extra burr phenomena, without bad appearance defect hidden danger, and swashs Photoetch has the characteristics such as non-contact, pollution-free, easy to control, is the important application skill of current conductive paste stockline etching width control Art.Since the conducting wire track using silk-screen printing technique is wider than 50 microns, and it is of less demanding to the dispersibility of silver powder, this Class silver powder has realized production domesticization at present;And as touch screen is thinner and lighter, the development of multi-touch function, to silver wire conducting wire cloth Line density proposes requirements at the higher level (20-30 μm of conductive line width), has exceeded the limitation of traditional silk-screened technology, therefore to silver powder More stringent requirements are proposed, that is, requires that the particle size range of silver powder is narrow, dispersion performance is good, is not allow for the presence of bulky grain silver powder, Otherwise it will affect the yields of touch screen, and the silver powder of China's laser-induced thermal etching has 90% or more to rely on import.
Summary of the invention
The object of the present invention is to provide a kind of touch screen preparation methods of laser ablation silver paste silver powder, to solve silver powder The more difficult concentration of partial size, size particles are unable to control, the bad problem of the dispersibility of silver powder.
In order to achieve the above object, the technical solution adopted by the present invention are as follows:
A kind of preparation method of touch screen laser ablation silver paste silver powder, it is characterised in that include the following steps:
Step 1: dissolving reduce agent in pure water, reducing agent solution A is obtained, temperature adjustment is to 45 ± 5 DEG C;
Step 2: dispersing agent is dissolved in pure water, adds alkali to adjust pH value to 12.0-13.0, obtain dispersant solution B, temperature adjustment is extremely 45±5℃;
Metal salt solution C is obtained Step 3: silver nitrate is dissolved in pure water, temperature adjustment is to 45 ± 5 DEG C;
Step 4: the dispersant solution B that step 2 the obtains and metal salt solution C that step 3 obtains is added what step 1 obtained It is stirred in reducing agent solution A, reacts 3-5min;
Step 5: being filtered after separation of solid and liquid when the mixed solution that step 4 is obtained is washed to filtered solution conductivity≤20ms Hydrophobicity auxiliary agent is added in filter cake, terminates to be dried to obtain silver powder when being dried to moisture content less than 0.2% for cake.
Reducing agent described in step 1 is formic acid, ascorbic acid, formaldehyde or hydrazine hydrate.
Alkali described in step 2 is sodium hydroxide, ammonium hydroxide or carbonic acid sodium.
Dispersing agent described in step 2 is benzotriazole acid, polyvinylpyrrolidone or Tween-80.
The concentration of silver nitrate described in step 3 is 600g/L-650g/L.
Step 1: reducing agent solution described in two, three, dispersant solution, silver nitrate solution temperature are 45 DEG C, it is to guarantee Reaction system initial temperature is 45 DEG C.Reaction temperature is higher than silver powder prepared by this temperature and is easy to reunite, and is lower than this thermotonus It is difficult to carry out completely.
Dispersant solution B described in step 4 and metal salt solution C are the reducing agent solution A being quickly poured under stirring In, the molar ratio of reducing agent and silver nitrate in the reducing agent solution A is 2:1-4:1, the dispersing agent in dispersant solution B with The molar ratio of silver nitrate is 0.01:1-0.05:1.
Hydrophobicity auxiliary agent described in step 5 is isomery stearic acid, hexadecanol, oleic acid or lauric acid, and hydrophobicity auxiliary agent is added Amount and the molar ratio of silver nitrate are 0.01:1-0.05:1.
The dispersant solution B and metal salt solution C time that reducing agent solution A is added is controlled in 10s described in step 4 It is interior.
The present invention having the beneficial effect that compared to the prior art
The present invention, which is used, adds dispersing agent into reducing agent solution, and adjusts reduction system pH value by the way that alkali is added to restore Metal salt solution C, obtains silver powder.The selection of reducing agent is satisfactory to obtain size in order to preferably control reaction rate Silver powder particles, the selection of dispersing agent are that silver powder is reunited during the preparation process in order to prevent, influence the pattern and physics and chemistry of silver powder Index, while the pH of reduction system is controlled, to guarantee the best use effect of reducing agent and dispersing agent, finally prepare silver powder grain Diameter is concentrated, size particles are controllable, silver powder good dispersion reaches acquisition crystallinity by control silver powder forming core and growth rate The purpose of high, homogeneous grain diameter silver powder product.
Preparation method of the invention is easy to operate, and raw material sources are extensive, at low cost, to the of less demanding of equipment;It obtains Touch screen is very high with the diameter of particle concentration degree of the preparation method of laser ablation silver paste silver powder, silver powder maximum particle diameter D1005 μ of < M, good dispersion.
Specific embodiment
The present invention will be further described With reference to embodiment.
A kind of touch screen preparation method of laser ablation silver paste silver powder, includes the following steps:
Step 1: dissolving reduce agent in pure water, reducing agent solution A is obtained, temperature adjustment is to 45 ± 5 DEG C;
Step 2: dispersing agent is dissolved in pure water, adds alkali to adjust pH value to 12.0-13.0, obtain dispersant solution B, temperature adjustment is extremely 45±5℃;
Metal salt solution C is obtained Step 3: silver nitrate is dissolved in pure water, temperature adjustment is to 45 ± 5 DEG C;
Step 4: the dispersant solution B that step 2 the obtains and metal salt solution C that step 3 obtains is added what step 1 obtained It is stirred in reducing agent solution A, reacts 3-5min;
Step 5: being filtered after separation of solid and liquid when the mixed solution that step 4 is obtained is washed to filtered solution conductivity≤20ms Hydrophobicity auxiliary agent is added in filter cake, terminates to be dried to obtain silver powder when being dried to moisture content less than 0.2% for cake.
Reducing agent described in step 1 is formic acid, ascorbic acid, formaldehyde or hydrazine hydrate.
Alkali described in step 2 is sodium hydroxide, ammonium hydroxide or carbonic acid sodium.
Dispersing agent described in step 2 is benzotriazole, polyvinylpyrrolidone or Tween-80.
The concentration of silver nitrate described in step 3 is 600g/L-650g/L.
Step 1: reducing agent solution described in two, three, dispersant solution, silver nitrate solution temperature are 45 DEG C, it is to guarantee Reaction system initial temperature is 45 DEG C.
Dispersant solution B described in step 4 and metal salt solution C are the reducing agent solution A being quickly poured under stirring In, the molar ratio of reducing agent and silver nitrate in the reducing agent solution A is 2:1-4:1, the dispersing agent in dispersant solution B with The molar ratio of silver nitrate is 0.01:1-0.05:1.
Hydrophobicity auxiliary agent described in step 5 is isomery stearic acid, hexadecanol, oleic acid or lauric acid, and hydrophobicity auxiliary agent is added Amount and the molar ratio of silver nitrate are 0.01:1-0.05:1.
The dispersant solution B and metal salt solution C time that reducing agent solution A is added is controlled in 10s described in step 4 It is interior.
Embodiment 1:
It weighs 176.82g hydrazine hydrate and is dissolved in spare in 1L pure water, as reducing agent solution A, temperature adjustment is to 45 DEG C;
Weigh 68g sodium hydroxide, 2.10g benzotriazole acid is dissolved in spare in 1L pure water, as dispersant solution B, temperature adjustment is extremely 45℃;
It weighs 300g silver nitrate and is dissolved in 0.5L water, as metal salt solution C, temperature adjustment is to 45 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 3min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Acquired solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, carries out solid-liquid Separation and filtering, are added 0.95g isomery stearic acid in filter cake Ag powder, 60 DEG C of 16 hours of drying to moisture content less than 0.2% after tie Beam is dry;
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 3.85 μm, tap density for 0.46 μm, D100 For 3.85g/cm3Touch screen laser ablation silver paste silver powder.
Embodiment 2:
It weighs 527.23g ascorbic acid and is dissolved in spare in 3.2L pure water, as reducing agent solution A, temperature adjustment is to 50 DEG C;
Weigh 216g sodium hydroxide, 1.75g benzotriazole acid be dissolved in it is spare in 3.2L water, extremely as dispersant solution B temperature adjustment 50℃;
It weighs 250g silver nitrate and is dissolved in 0.4 L water, as metal salt solution C, temperature adjustment is to 50 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 5min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Obtained solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, consolidate Liquid separates and filtering, 1.59g isomery stearic acid is added in filter cake Ag powder, after 60 DEG C of 18 hours of drying to moisture content are less than 0.2% Terminate drying.
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 3.97 μm, jolt ramming for 0.51 μm, D100 Density is 3.15g/cm3Touch screen laser ablation silver paste silver powder.
Embodiment 3:
It weighs 528.40 formic acid and is dissolved in spare in 3L pure water, as reducing agent solution A, temperature adjustment is to 40 DEG C;
Weigh 150g sodium hydroxide, 34.19g benzotriazole acid is dissolved in spare in 2L water, as dispersant solution B, temperature adjustment is extremely 40℃;
It weighs 975g silver nitrate and is dissolved in 1.5L water, as metal salt solution C, temperature adjustment is to 40 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 5min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Obtained solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, consolidate Liquid separation and filtering, are added 6.18g isomery stearic acid in filter cake Ag powder, 60 DEG C drying 20 hours to moisture content less than 0.2% after tie Beam is dry.
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 3.53 μm, jolt ramming for 0.49 μm, D100 Density is 3.5g/cm3Touch screen laser ablation silver paste silver powder.
Embodiment 4:
It weighs 530.35 formaldehyde and is dissolved in spare in 3L pure water, as reducing agent solution A, temperature adjustment is to 45 DEG C;
Weigh 130g sodium hydroxide, 7.01g benzotriazole acid be dissolved in it is spare in 2L water, as dispersant solution B, temperature adjustment to 45 ℃;
It weighs 1000g silver nitrate and is dissolved in 1.7L water, as metal salt solution C, temperature adjustment is to 45 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 4min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Obtained solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, consolidate Liquid separation and filtering, are added 3.16g isomery stearic acid in filter cake Ag powder, 60 DEG C drying 16 hours to moisture content less than 0.2% after tie Beam is dry.
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 3.13 μm, jolt ramming for 0.43 μm, D100 Density is 2.9g/cm3Touch screen laser ablation silver paste silver powder.
Embodiment 5:
It weighs 588 hydrazine hydrates and is dissolved in spare in 3L pure water, as reducing agent solution A, temperature adjustment is to 45 DEG C;
Weigh 177g sodium bicarbonate, 500g polyvinylpyrrolidone is dissolved in spare in 2L water, as dispersant solution B, temperature adjustment is extremely 45℃;
It weighs 1000g silver nitrate and is dissolved in 1.5 L water, as metal salt solution C, temperature adjustment is to 45 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 4min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Obtained solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, consolidate Liquid separation and filtering, are added 14g hexadecanol in filter cake Ag powder, 60 DEG C drying 16 hours to moisture content less than 0.2% after terminate it is dry It is dry.
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 2.13 μm, vibration density for 0.5 μm, D100 Degree is 4.5g/cm3Touch screen laser ablation silver paste silver powder.
Embodiment 6:
It weighs 635 formaldehyde and is dissolved in spare in 3L pure water, as reducing agent solution A, temperature adjustment is to 45 DEG C;
Weigh 125g ammonium hydroxide, 50g Tween-80 is dissolved in spare in 2L water, as dispersant solution B, temperature adjustment is to 45 DEG C;
It weighs 1000g silver nitrate and is dissolved in 1.7 L water, as metal salt solution C, temperature adjustment is to 45 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 4min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Obtained solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, consolidate Liquid separation and filtering, are added 33g oleic acid in filter cake Ag powder, 60 DEG C drying 16 hours to moisture content less than 0.2% after terminate drying.
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 4.39 μm, jolt ramming for 0.58 μm, D100 Density is 3.5g/cm3Touch screen laser ablation silver paste silver powder.
Embodiment 7:
It weighs 600 formaldehyde and is dissolved in spare in 3L pure water, as reducing agent solution A, temperature adjustment is to 45 DEG C;
Weigh 150g ammonium hydroxide, 60g Tween-80 is dissolved in spare in 2L water, as dispersant solution B, temperature adjustment is to 45 DEG C;
It weighs 1000g silver nitrate and is dissolved in 1.5 L water, as metal salt solution C, temperature adjustment is to 45 DEG C;
Dispersant solution B, metal salt solution C are quickly poured into the lower reducing agent solution A of stirring and reacted, is controlled and is poured into the time and exist It within 10s, and is stirred, dispersant solution B reacts 4min after all pouring into, detect in reaction solution without Ag+When determine reaction Terminate;
Obtained solution is separated by solid-liquid separation and is filtered, when conductivity≤20ms washed several times to filtered solution, consolidate Liquid separation and filtering, are added 25g lauric acid in filter cake Ag powder, 60 DEG C drying 16 hours to moisture content less than 0.2% after terminate it is dry It is dry.
300 mesh sieve of obtained silver powder are sieved, obtain D after screening50It is 4.66 μm, jolt ramming for 0.91 μm, D100 Density is 3.57g/cm3Touch screen laser ablation silver paste silver powder.

Claims (8)

1. a kind of touch screen preparation method of laser ablation silver paste silver powder, it is characterised in that include the following steps:
Step 1: dissolving reduce agent in pure water, reducing agent solution A is obtained, temperature adjustment is to 45 ± 5 DEG C;
Step 2: dispersing agent is dissolved in pure water, adds alkali to adjust pH value to 12.0-13.0, obtain dispersant solution B, temperature adjustment is extremely 45±5℃;
Metal salt solution C is obtained Step 3: silver nitrate is dissolved in pure water, temperature adjustment is to 45 ± 5 DEG C;
Step 4: the dispersant solution B that step 2 the obtains and metal salt solution C that step 3 obtains is added what step 1 obtained It is stirred in reducing agent solution A, reacts 3-5min;
Step 5: being filtered after separation of solid and liquid when the mixed solution that step 4 is obtained is washed to filtered solution conductivity≤20ms Hydrophobicity auxiliary agent is added in filter cake, terminates to be dried to obtain silver powder when being dried to moisture content less than 0.2% for cake.
2. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 1 Described in reducing agent be formic acid, ascorbic acid, formaldehyde or hydrazine hydrate.
3. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 2 Described in alkali be sodium hydroxide, ammonium hydroxide or carbonic acid sodium.
4. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 2 Described in dispersing agent be benzotriazole acid, polyvinylpyrrolidone or Tween-80.
5. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 3 Described in silver nitrate concentration be 600g/L-650g/L.
6. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 4 Described in dispersant solution B and metal salt solution C be quickly poured into stirring under reducing agent solution A in, the reducing agent is molten The molar ratio of reducing agent and silver nitrate in liquid A is 2:1-4:1, the molar ratio of dispersing agent and silver nitrate in dispersant solution B For 0.01:1-0.05:1.
7. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 5 Described in hydrophobicity auxiliary agent be isomery stearic acid, hexadecanol, oleic acid or lauric acid, hydrophobicity promoter addition and silver nitrate rub You are than being 0.01:1-0.05:1.
8. the touch screen as described in claim 1 preparation method of laser ablation silver paste silver powder, it is characterised in that: step 4 Described in dispersant solution B and metal salt solution the C time that reducing agent solution A is added are controlled in 10s.
CN201810886037.7A 2018-08-06 2018-08-06 A kind of preparation method of touch screen laser ablation silver paste silver powder Pending CN109014239A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810886037.7A CN109014239A (en) 2018-08-06 2018-08-06 A kind of preparation method of touch screen laser ablation silver paste silver powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810886037.7A CN109014239A (en) 2018-08-06 2018-08-06 A kind of preparation method of touch screen laser ablation silver paste silver powder

Publications (1)

Publication Number Publication Date
CN109014239A true CN109014239A (en) 2018-12-18

Family

ID=64649758

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810886037.7A Pending CN109014239A (en) 2018-08-06 2018-08-06 A kind of preparation method of touch screen laser ablation silver paste silver powder

Country Status (1)

Country Link
CN (1) CN109014239A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110202164A (en) * 2019-06-06 2019-09-06 河南金渠银通金属材料有限公司 A kind of nano-silver powder and preparation method thereof for electric source material
CN110586959A (en) * 2019-10-28 2019-12-20 苏州银瑞光电材料科技有限公司 Preparation method of flake silver powder with high tap density
CN111438369A (en) * 2019-01-16 2020-07-24 北京氦舶科技有限责任公司 Silver powder, preparation method thereof and laser etching silver paste
CN112091233A (en) * 2020-11-19 2020-12-18 西安宏星电子浆料科技股份有限公司 Synthesis method of silver nanoparticles
CN112974827A (en) * 2019-12-12 2021-06-18 长沙理工大学 Preparation method of spherical silver powder with high tap density and surface wrinkles
CN113290252A (en) * 2021-05-28 2021-08-24 金川集团股份有限公司 Preparation method of superfine silver powder with low tap mass and high specific surface
CN114951678A (en) * 2022-04-25 2022-08-30 金川集团股份有限公司 Preparation method of spherical superfine silver powder for silver paste on front surface of solar cell

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102962473A (en) * 2012-12-06 2013-03-13 云南铜业科技发展股份有限公司 Method for preparing silver powder for touch screen silver paste
CN105081343A (en) * 2015-08-03 2015-11-25 佛山市顺德区百锐新电子材料有限公司 Manufacturing method for conductive silver powder used for touch screen UV-type laser engraving silver paste
CN106862588A (en) * 2017-01-23 2017-06-20 湖南省国银新材料有限公司 A kind of preparation method of laser engraving touch-screen silver paste super fine silver powder
CN107876799A (en) * 2017-12-18 2018-04-06 西安宏星电子浆料科技有限责任公司 High-tap density low specific surface area super fine silver powder and preparation method thereof
CN107971502A (en) * 2017-11-01 2018-05-01 昆明理工大学 A kind of preparation method of high dispersiveness spherical silver powder

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102962473A (en) * 2012-12-06 2013-03-13 云南铜业科技发展股份有限公司 Method for preparing silver powder for touch screen silver paste
CN105081343A (en) * 2015-08-03 2015-11-25 佛山市顺德区百锐新电子材料有限公司 Manufacturing method for conductive silver powder used for touch screen UV-type laser engraving silver paste
CN106862588A (en) * 2017-01-23 2017-06-20 湖南省国银新材料有限公司 A kind of preparation method of laser engraving touch-screen silver paste super fine silver powder
CN107971502A (en) * 2017-11-01 2018-05-01 昆明理工大学 A kind of preparation method of high dispersiveness spherical silver powder
CN107876799A (en) * 2017-12-18 2018-04-06 西安宏星电子浆料科技有限责任公司 High-tap density low specific surface area super fine silver powder and preparation method thereof

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111438369A (en) * 2019-01-16 2020-07-24 北京氦舶科技有限责任公司 Silver powder, preparation method thereof and laser etching silver paste
CN110202164A (en) * 2019-06-06 2019-09-06 河南金渠银通金属材料有限公司 A kind of nano-silver powder and preparation method thereof for electric source material
CN110586959A (en) * 2019-10-28 2019-12-20 苏州银瑞光电材料科技有限公司 Preparation method of flake silver powder with high tap density
CN112974827A (en) * 2019-12-12 2021-06-18 长沙理工大学 Preparation method of spherical silver powder with high tap density and surface wrinkles
CN112091233A (en) * 2020-11-19 2020-12-18 西安宏星电子浆料科技股份有限公司 Synthesis method of silver nanoparticles
CN113290252A (en) * 2021-05-28 2021-08-24 金川集团股份有限公司 Preparation method of superfine silver powder with low tap mass and high specific surface
CN114951678A (en) * 2022-04-25 2022-08-30 金川集团股份有限公司 Preparation method of spherical superfine silver powder for silver paste on front surface of solar cell
CN114951678B (en) * 2022-04-25 2023-12-26 金川集团股份有限公司 Preparation method of spherical superfine silver powder for front silver paste of solar cell

Similar Documents

Publication Publication Date Title
CN109014239A (en) A kind of preparation method of touch screen laser ablation silver paste silver powder
US8231704B2 (en) Silver particles and processes for making them
US8366799B2 (en) Silver particles and a process for making them
US8372178B2 (en) Silver particles and processes for making them
CN101195170A (en) Method for preparing superfine copper powder
JPWO2014104032A1 (en) Method for producing copper powder, copper powder and copper paste
CN102554219A (en) Nanoparticle of copper-tin nuclear shell structure and preparation method for nanoparticle
CN108907226A (en) A kind of preparation method for laser ablation electrode circuit super fine silver powder
EP1839784A1 (en) Nickel powder, process for producing the same, and conductive paste
CN101830498A (en) Preparation method of ITO (Indium Tin Oxide) powder and ITO sintering body
CN105788703B (en) A kind of anti-oxidant silver-bearing copper slurry for being used to be electromagnetically shielded and preparation method thereof
CN114029499B (en) Preparation method of ultralong nano silver wire material
CN109423636A (en) A kind of preparation method of secondary silver-plated highly conductive filler
CN109692971A (en) A kind of nano-silver powder and its preparation and the application in low-temperature cured conductive silver paste
CN109401442A (en) A kind of silver-plated electrically conductive ink of UV curing nano and preparation method thereof
JP2007169770A (en) Copper powder, copper particle and method for producing the copper particle
CN102941351A (en) Preparation method of superfine copper powder
CN103737011B (en) The preparation method of high compaction spherical silver powder
CN114939668A (en) Preparation method of superfine silver powder and silver conductive paste thereof
CN105081343B (en) A kind of manufacture method of conductive silver powder for touch-screen UV type laser engraving silver pastes
CN104672991B (en) A kind of preparation method of copper conductive ink
CN106519302A (en) Laser-forming plastic active additive and preparation method thereof
CN105170996A (en) Preparation method of ultrafine copper powder for chip multilayer ceramic capacitors
CN105817646B (en) A kind of preparation method of the ball shape silver powder of high-tap density
CN104493175B (en) A kind of preparation method of the siller tin oxide electric contact material containing additive

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20181218